ENST00000697149.1:c.1599A>G
|
ENSP00000513138.1:n.1599A>G
|
|
ENST00000697150.1:c.1657A>G
|
ENSP00000513139.1:n.1657A>G
|
|
ENST00000697151.1:c.1590A>G
|
ENSP00000513140.1:n.1590A>G
|
|
ENST00000697164.1:c.1670A>G
|
ENSP00000513153.1:p.Gln557Arg
|
|
ENST00000697165.1:c.1457A>G
|
ENSP00000513154.1:p.Gln486Arg
|
|
ENST00000347310.10:c.1760A>G
MANE Select
|
ENSP00000321345.5:p.Gln587Arg
|
|
ENST00000637002.1:c.1151A>G
|
ENSP00000490340.1:p.Gln384Arg
|
|
ENST00000347310.9:c.1760A>G
|
ENSP00000321345.5:p.Gln587Arg
|
|
ENST00000395227.2:c.554A>G
|
ENSP00000378652.2:p.Gln185Arg
|
|
ENST00000425614.3:c.995A>G
|
ENSP00000387640.2:p.Gln332Arg
|
|
ENST00000473881.2:c.*586A>G
|
ENSP00000486667.1:n.*586A>G
|
|
NM_144701.2:c.1760A>G
|
NP_653302.2:p.Gln587Arg
|
|
XM_005270516.2:c.998A>G
|
XP_005270573.1:p.Gln333Arg
|
|
XM_011540789.1:c.1850A>G
|
XP_011539091.1:p.Gln617Arg
|
|
XM_011540790.1:c.1760A>G
|
XP_011539092.1:p.Gln587Arg
|
|
XM_011540791.1:c.1760A>G
|
XP_011539093.1:p.Gln587Arg
|
|
XM_011540790.3:c.1760A>G
|
XP_011539092.1:p.Gln587Arg
|
|
XM_011540791.3:c.1760A>G
|
XP_011539093.1:p.Gln587Arg
|
|
XR_001736993.1:n.1840A>G
|
|
|
NM_144701.3:c.1760A>G
MANE Select
|
NP_653302.2:p.Gln587Arg
|
|